Abstract
BackgroundAlpha-lipoic acid (aLA) is a strong antioxidant commonly used for treating diabetic polyneuropathy. Previously, we demonstrated the neurorestorative effects of aLA after cerebral ischemia in rats. However, its effects on patients with stroke remain unknown. We investigated whether patients treated with aLA have better functional outcomes after acute ischemic stroke (AIS) and reperfusion therapy than patients not receiving aLA.MethodsIn this retrospective study of 172 prospectively registered patients with diabetes and AIS treated with tissue plasminogen activator (tPA), we investigated the relationship between aLA use and functional outcome both after 3 months and after 1 year. The functional outcomes included occurrence of hemorrhagic transformation (HT), early neurological deterioration (END), and early clinical improvement (ECI). Favorable outcomes were defined as modified Rankin Scale (mRS) scores of 0–2.ResultsOf the 172 patients with AIS and diabetes, 47 (27.3%) used aLA. In the entire cohort, favorable outcomes occurred at significantly higher rates both at 3 months and at 1 year in those treated with aLA. The risks for END and HT were lower and the occurrence of ECI was higher in patients treated with aLA. In multivariable analysis, aLA use was associated with favorable outcomes both at 3 months and at 1 year. Age, HT, and increased National Institutes of Health Stroke Scale scores were negative predictors of a favorable outcome.ConclusionsThe use of aLA in patients with AIS and diabetes who are treated with tPA is associated with favorable outcomes. These results indicate that aLA could be a useful intervention for the treatment of AIS after reperfusion therapy.
Highlights
Despite significant advances in the prevention and treatment of stroke, it is still one of the leading causes of death and debilitating disease
In this retrospective study of 172 prospectively registered patients with diabetes and acute ischemic stroke (AIS) treated with tissue plasminogen activator, we investigated the relationship between Alpha-lipoic acid (aLA) use and functional outcome both after 3 months and after 1 year
Favorable outcomes occurred at significantly higher rates both at 3 months and at 1 year in those treated with aLA
Summary
Despite significant advances in the prevention and treatment of stroke, it is still one of the leading causes of death and debilitating disease. It is reported that there are no pharmacological agents with putative neuroprotective actions that have demonstrated efficacy in improving outcomes after ischemic stroke in humans [1]. There is a clear need for research to discover potential neuroprotective agents and new therapeutic strategies. The increased delivery of oxygen to ischemic brain tissue after reperfusion therapy may promote oxidative stress and cell death due to an increase in free radical generation [4]. The use of antioxidants should be a promising strategy for treating ischemia-reperfusion injury. We demonstrated the neurorestorative effects of aLA after cerebral ischemia in rats. We investigated whether patients treated with aLA have better functional outcomes after acute ischemic stroke (AIS) and reperfusion therapy than patients not receiving aLA
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